17 Pharmaceutical Regulatory Compliance Jobs in Norwood, MA
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QC Micro Associate Randstad USA - Norwood, MA, United States , Massachusetts. What you will be doing: Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements. Execute tasks precisely as defined 19 days ago
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Senior Clinical Trial Associate ONO PHARMA USA - Cambridge, MA, United States of the Pharmaceutical Industry Clinical trial process (clinical trial conduct, documentation and reporting) in accordance with ICH/GCP and other regulatory compliance guidelines. Cognitive Skills Problem solving 8 days ago
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Medical Science Liaison, New York City/ Boston, MA Boston, MA hematology/oncology experience is strongly preferred. Clinical research experience is preferred. Knowledge of applicable treatment, compliance, and regulatory guidelines. Excellent interpersonal communication 6 days ago
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Director of Quality Assurance Albion Rye Associates - Boston, MA, United States regulatory requirements is a plus Solid well-grounded experience in GXP compliance including knowledge and experience in preparation of Clinical sections of INDs, CTAs, BLAs, MAAs and NDSs submissions 8 days ago
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Quality Control Laboratory Manager Tedor Pharma Services - Cumberland, RI, United States environment. Solid understanding of GMP compliance, Quality Control CMC requirements for ANDAs, and other regulatory filings Excellent interpersonal, verbal, and written communication skills Demonstrated 11 days ago
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Medical Science Liaison Incyte Corporation - Boston, Massachusetts, USA hematology/oncology experience is strongly preferred. Clinical research experience is preferred. Knowledge of applicable treatment, compliance, and regulatory guidelines. Excellent interpersonal communication 9 days ago
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Principal Specialist, Quality Assurance Operations - 2483 Editas Medicine - Cambridge, MA . Understanding of regulatory guidance on cell and gene therapy products. Expertise working within cGMP compliance and providing GMP documentation. Preferred Qualifications: Additionally, candidates More than 30 days ago
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Director of Clinical Operations Global Life Science Hub - Boston, MA and collaborations. Collaborate closely with Quality Management to ensure ongoing compliance and regulatory adherence. Qualifications: Bachelor's degree in life sciences or related field; advanced degree preferred. 10 200,000 - 225,000 19 days ago
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Senior Director, Medical Writing Ironwood Pharmaceuticals - Boston, Massachusetts, USA , as applicable. Participate in the development of department SOPs and process-related tools to improve and enhance operations and to ensure compliance with regulatory standards and ICH/GCP/eCTD guidelines. Support $239,000 to $278,565 26 days ago
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Senior Quality Assurance Consultant LS Solutions - Cambridge, MA in quality assurance and regulatory compliance in the pharmaceutical and medical device sectors. Expertise in cell therapy manufacturing, cloud-based data management systems, and medical device remediation More than 30 days ago
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